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4-Aminofluoren-9-one

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Identification
Molecular formula
C13H9NO
CAS number
2834-85-5
IUPAC name
4-aminofluoren-9-one
State
State

At room temperature, 4-Aminofluoren-9-one is in a solid state, typically observed as a powder.

Melting point (Celsius)
226.00
Melting point (Kelvin)
499.15
Boiling point (Celsius)
475.00
Boiling point (Kelvin)
748.15
General information
Molecular weight
195.22g/mol
Molar mass
195.2220g/mol
Density
1.2460g/cm3
Appearence

4-Aminofluoren-9-one typically appears as a pale yellow to yellow crystalline powder. It is noted for its crystalline structure which can be highlighted under light, often giving a glistening effect.

Comment on solubility

Solubility of 4-Aminofluoren-9-one

The solubility of 4-aminofluoren-9-one, a compound with the formula C13H11N1O, is influenced by several factors that determine its behavior in various solvents.

General Solubility Characteristics:

  • Polar solvents: 4-aminofluoren-9-one is generally poorly soluble in polar solvents such as water. This is due to the relative hydrophobic nature of its aromatic structure.
  • Non-polar solvents: It demonstrates better solubility in non-polar or slightly polar solvents like chloroform and benzene, which can stabilize the aromatic π-system.
  • Temperature effects: Solubility may increase with temperature due to enhanced molecular motion, allowing for greater interaction with the solvent.

In summary, while 4-aminofluoren-9-one is not very soluble in water, it shows a propensity to dissolve in non-polar organic solvents, making it more accessible for use in organic reactions. As with many organic compounds, solubility is a key factor in determining the compound's reactivity and potential applications.

Interesting facts

Interesting Facts about 4-Aminofluoren-9-one

4-Aminofluoren-9-one, often referred to as an important organic compound in various chemical syntheses, has garnered attention due to its unique properties and versatile applications. Here are some notable highlights:

  • Structure and Stability: With a molecular structure featuring both an amine and a ketone functional group, 4-Aminofluoren-9-one is a great example of how structural diversity can influence the chemical behavior of compounds.
  • Colorimetric Applications: This compound is significant in analytical chemistry as it serves as a chromogenic agent. It is often used in the detection of specific analytes due to its ability to change color in reaction conditions, making it a valuable tool in laboratory settings.
  • Fluorescent Properties: The presence of the fluorenone moiety contributes to its fluorescent properties, which are exploited in both research and industrial applications for detecting light in various samples.
  • Biochemical Relevance: Research has indicated that 4-Aminofluoren-9-one may play a role in studies surrounding biochemical pathways, particularly those involving the metabolism of certain drugs and environmental pollutants.

As a compound, 4-Aminofluoren-9-one represents a fascinating intertwining of organic chemistry and practical applications. Its properties not only underscore the versatility of organic compounds in overcoming analytical challenges but also highlight the importance of research in developing methods that reveal intricate details of chemical behavior. Indeed, as researchers quote, "In the world of chemistry, every compound tells a story."

Understanding and harnessing the potential of this compound can lead to significant advancements in synthetic organic chemistry and analytical techniques.

Synonyms
4-Amino-9-fluorenone
4269-15-2
4-Amino-9H-fluoren-9-one
4-Aminofluorenone
FLUOREN-9-ONE, 4-AMINO-
9H-Fluoren-9-one, 4-amino-
EINECS 224-257-5
1O6X3ML5IP
NSC 22836
BRN 2804575
NSC-22836
DTXSID80195387
4-14-00-00313 (Beilstein Handbook Reference)
DTXCID90117878
224-257-5
4-aminofluoren-9-one
4-Amino-fluorenon
NSC22836
4-amino-fluoren-9-one
UNII-1O6X3ML5IP
4-Amino-9-fluorenone, 95%
CHEMBL386818
SCHEMBL1143189
4-Amino-9H-fluoren-9-one #
FFWCEONGEXZNFU-UHFFFAOYSA-
AKOS015894713
NS00031224
InChI=1/C13H9NO/c14-11-7-3-6-10-12(11)8-4-1-2-5-9(8)13(10)15/h1-7H,14H2